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Genetic instability of Japanese encephalitis virus cDNA clones propagated in Escherichia coli

机译:在大肠杆菌中繁殖的日本脑炎病毒cDNA克隆的遗传不稳定性

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The genetic instability of Flavivirus cDNA clones in transformed bacteria is a common phenomenon. Herein, a cDNA fragment of the nucleotide (nt) 1-2913 of the genome of a flavivirus, Japanese encephalitis virus (JEV), was used to investigate factors that caused the instability of cDNA clones. Several cDNA fragments with different 5'- or 3'-termini of the 2913-nt cDNA were obtained by PCR amplification or restriction enzyme digestion and cloned into a pCR-Blunt II-TOPO vector. All the cDNA fragments were stably propagated at 25 A degrees C. However, the 5'-untranslated region and half of the 3'-E gene could cause the instability of the 2913-nt cDNA at 37 A degrees C. The 5'-terminus sequences of the 2913-nt fragment were subjected to testing of the prokaryotic promoter activity by luciferase assay and Western blot. The sequences of 54-120 nt of the JEV genome exhibited high prokaryotic promoter activity at 37 A degrees C, and the activity declined markedly at 25 A degrees C. These findings revealed that the high prokaryotic promoter activity of the 54-120 nt sequences of the JEV genome together with expression of JEV structural genes determined the instability of a JEV cDNA clone. Growth at room temperature may reduce the prokaryotic promoter activity of 5'-sequences of the JEV genome and could represent an effective way to improve the stability of flavivirus cDNA clones in host bacteria.
机译:黄杆菌病毒cDNA克隆在转化细菌中的遗传不稳定性是普遍现象。本文中,黄病毒日本脑炎病毒(JEV)的黄病毒基因组核苷酸(nt)1-2913的cDNA片段用于研究引起cDNA克隆不稳定的因素。通过PCR扩增或限制性内切酶消化获得了具有不同的2913-nt cDNA 5'-或3'-末端的cDNA片段,并将其克隆到pCR-Blunt II-TOPO载体中。所有cDNA片段均在25 A摄氏度下稳定繁殖。但是,5'-非翻译区和3'-E基因的一半可能会导致2913-nt cDNA在37 A摄氏度下不稳定。5'-通过荧光素酶测定和Western印迹对2913-nt片段的末端序列进行原核启动子活性的测试。 JEV基因组54-120 nt的序列在37 A时表现出高原核启动子活性,而在25 A时该活性显着​​下降。这些发现表明,JEV基因组的54-120 nt序列的原核启动子活性很高。 JEV基因组以及JEV结构基因的表达决定了JEV cDNA克隆的不稳定性。在室温下生长可能会降低JEV基因组5'序列的原核启动子活性,并且可能代表一种改善黄病毒cDNA克隆在宿主细菌中稳定性的有效方法。

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